ORPHA:294023
Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:294023 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Blepharitis
- Onychogryphosis
- Psoriasiform dermatitis
- Recurrent bacterial skin infections
- Chronic monilial nail infection
- Erythema